Definition of neonatal sepsis,type of neonatal sepsis ,early onset neonatal sepsis,late onset neonatal sepsis,Pathophysiology of neonatal sepsis,,sign and symptoms of neonatal sepsis, diagnosis of neonatal sepsis,management of neonatal sepsis, antibiotic used for neonatal sepsis,prevention of neonatal sepsis, prognosis of neonatal sepsis ,and A summary
Definition of neonatal sepsis,type of neonatal sepsis ,early onset neonatal sepsis,late onset neonatal sepsis,Pathophysiology of neonatal sepsis,,sign and symptoms of neonatal sepsis, diagnosis of neonatal sepsis,management of neonatal sepsis, antibiotic used for neonatal sepsis,prevention of neonatal sepsis, prognosis of neonatal sepsis ,and A summary
This was done as a student presentation using photographs & content from various web sites & textbooks on the assumption of fair usage for studying & is for NON-COMMERCIAL purposes.
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thrombotic complication in neonate is quite higher as compared to paediatric age group ,so early detection with sign and symptoms ,early estb.of diagnosis is very important and early treatment .there are long term complication of neonatal thrombosis ,we have to be aware of complications.
this ppt will might help in understanding the topic.
thanks .best of luck
Amniotic fluid maintain the perfect homeostasis between mother and fetus. It protect both mother and fetus from various complications. Details is enclosed in presentation.
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This short cheat book talks about basic concepts and physiology of artificial ventilation and also elaborates on point guided approach in maneuvering different modes of mechanical ventilation. Consider this as a basic overview and is intended for all internal medicine residents.
Salient features of the book are -
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Are you curious about what’s new in cervical cancer research or unsure what the findings mean? Join Dr. Emily Ko, a gynecologic oncologist at Penn Medicine, to learn about the latest updates from the Society of Gynecologic Oncology (SGO) 2024 Annual Meeting on Women’s Cancer. Dr. Ko will discuss what the research presented at the conference means for you and answer your questions about the new developments.
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This includes all relevant anatomy and clinical tests compiled from standard textbooks, Campbell,netter etc..It is comprehensive and best suited for orthopaedicians and orthopaedic residents.
Basavarajeeyam is an important text for ayurvedic physician belonging to andhra pradehs. It is a popular compendium in various parts of our country as well as in andhra pradesh. The content of the text was presented in sanskrit and telugu language (Bilingual). One of the most famous book in ayurvedic pharmaceutics and therapeutics. This book contains 25 chapters called as prakaranas. Many rasaoushadis were explained, pioneer of dhatu druti, nadi pareeksha, mutra pareeksha etc. Belongs to the period of 15-16 century. New diseases like upadamsha, phiranga rogas are explained.
Recomendações da OMS sobre cuidados maternos e neonatais para uma experiência pós-natal positiva.
Em consonância com os ODS – Objetivos do Desenvolvimento Sustentável e a Estratégia Global para a Saúde das Mulheres, Crianças e Adolescentes, e aplicando uma abordagem baseada nos direitos humanos, os esforços de cuidados pós-natais devem expandir-se para além da cobertura e da simples sobrevivência, de modo a incluir cuidados de qualidade.
Estas diretrizes visam melhorar a qualidade dos cuidados pós-natais essenciais e de rotina prestados às mulheres e aos recém-nascidos, com o objetivo final de melhorar a saúde e o bem-estar materno e neonatal.
Uma “experiência pós-natal positiva” é um resultado importante para todas as mulheres que dão à luz e para os seus recém-nascidos, estabelecendo as bases para a melhoria da saúde e do bem-estar a curto e longo prazo. Uma experiência pós-natal positiva é definida como aquela em que as mulheres, pessoas que gestam, os recém-nascidos, os casais, os pais, os cuidadores e as famílias recebem informação consistente, garantia e apoio de profissionais de saúde motivados; e onde um sistema de saúde flexível e com recursos reconheça as necessidades das mulheres e dos bebês e respeite o seu contexto cultural.
Estas diretrizes consolidadas apresentam algumas recomendações novas e já bem fundamentadas sobre cuidados pós-natais de rotina para mulheres e neonatos que recebem cuidados no pós-parto em unidades de saúde ou na comunidade, independentemente dos recursos disponíveis.
É fornecido um conjunto abrangente de recomendações para cuidados durante o período puerperal, com ênfase nos cuidados essenciais que todas as mulheres e recém-nascidos devem receber, e com a devida atenção à qualidade dos cuidados; isto é, a entrega e a experiência do cuidado recebido. Estas diretrizes atualizam e ampliam as recomendações da OMS de 2014 sobre cuidados pós-natais da mãe e do recém-nascido e complementam as atuais diretrizes da OMS sobre a gestão de complicações pós-natais.
O estabelecimento da amamentação e o manejo das principais intercorrências é contemplada.
Recomendamos muito.
Vamos discutir essas recomendações no nosso curso de pós-graduação em Aleitamento no Instituto Ciclos.
Esta publicação só está disponível em inglês até o momento.
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TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
TEST BANK for Operations Management, 14th Edition by William J. Stevenson, Verified Chapters 1 - 19, Complete Newest Version.pdf
Thyroid Gland- Gross Anatomy by Dr. Rabia Inam Gandapore.pptx
Bleeding in newborns
1. Bleeding in Newborns
Dr. Kalpana Malla
MD Pediatrics
Manipal Teaching Hospital
Download more documents and slide shows on The Medical Post [ www.themedicalpost.net ]
2. Introduction
• Neonates are susceptible to bleeding for
various reasons
Immaturity of the haemostatic system
because of quantitative and qualitative
deficiency of coagulation factors
Maternal disease and drugs
Birth trauma
Other conditions - sepsis and asphyxia
3. Clinical presentation
• Bleeding in neonates may present with
Oozing from the umbilical stump
Cephalhaematoma
Bruising , Petechiae
Bleeding from peripheral venipuncture or
procedure sites
Bleeding into scalp
5. • A detailed history and examination essential
in the assessment of bleeding neonate
History includes
• Maternal diseases as ITP, preeclampsia and
diabetes
• Maternal exposure to drugs as
aspirin, anticonvulsants, rifampicin and
isoniazid
• Family history of bleeding disorders
• Previous affected siblings
8. Etiology
• Coagulation disorders - acquired
congenital
• Platelet disorders -thrombocytopenia
function defects
• Combination of above factors – DIC
• Defects in fibrinolytic pathway
• Trauma
9. Coagulation disorders
• Transient - Vitamin K deficiency
Maternal drug use
• Congenital - Autosomal dominant- vWF
X linked recessive – VIII,IX
Autosomal recessive – II,V,VII
10. Vitamin K deficiency
• VKD factors – Required for gamma
carboxylation of II, VII, IX, and X
• Causes – breast milk has low vit K
lack of gut flora
no placental transfer
11. VKDB
• Early , Classic, and Late forms
• Early VKDB – in first day
• Severe bleeding – GI and ICH
• Cause – Maternal drug intake
Phenytoin, phenobarb,
ATT, warfarin
12. VKDB
Classical form: 2-7 days of age
• 0.25-1.7% of all babies
• Cause – not received prophylaxis
on breast feeds, sterile gut, lack of
placental transfer
Late form : 2-8 weeks of age
• Boys > girls, 5-10/1 lac
• Well , breastfed, term baby
• Liver disease
• Malabsorption
13. Management of VKDB
• Prolonged PT , APTT (if severe)
• Normal platelets and fibrinogen
• PIVKA – half life of 70 hrs
• Factor assays of vit K dependent
factors
• Treatment – 1mg iv or sc
• FFP in severe cases and PCC
14. Prophylaxis of VKDB
• Early VKDB- single IM inj of vit K at
birth and oral Vit K to mother for
last 4 weeks
• Classical and Late forms –
IM Vit K at birth
oral Vit K at 0 , 4 days and 4 weeks
In preterms – Weekly iv Vit K
15. Hemophilia in the Newborn
• Factor VIII or XI deficiency
– A good family history goes a long way
16. Hemophilia A
• Most common inherited clotting factor def
• X linked recessive, 1 in 4000 males
• 1/3rd of cases present in newborn period
• ICH(25%), cephalhematoma(10-15%)
• Post circumcision bleed is characteristic
• Family history – absent in 30%
• Inv – prolonged APTT, normal PT, normal
platelets.
• Factor VIIIc assay level <2% severe, 2-10%
moderate, >10% mild
17. Hemophilia A
• Treatment – Factor VIII concentrates
50 -100 U/kg
• Raise level to 100%
• In ICH – factor infusion for 14 days
• In doubtful cases – cryoprecipitate or FFP
• Management of antenatally detected
cases:
- Avoid difficult delivery , oral Vit K
- Cord blood bleeding tests, factor VIII
- No role for prophylactic Factor VIII
19. Hemophilia B
• XLR
• Deficiency of Factor IX
• Less common than the classical form
• Prolonged APTT and low Factor IX
• Rx- 100u/k iv OD , to raise levels to 100%
• Avoid lumbar punctures, IM injections
20. Thrombocytopenia
• Less than 150,000/uL
• Incidence in newborns: 1-5%
• Incidence in NICU – 15-30%
• In VLBW and preterms – 50%
• Causes of thrombocytopenia in newborn:
Neonatal megakaryocytes are smaller
Inadequate production of thrombopoietin
24. Late Thrombocytopenia
• Late onset sepsis and NEC
• Congenital infection
• Maternal ITP, SLE
• Congenital / Inherited conditions
25. Infection
• Most common cause of thrombocytopenia
in infants
• LOS > EOS
• 50% of babies have platelets < 1 lac/cmm
• 65%, and 47% - sensitivity and specificity
for sepsis
• Viral infections ( intrauterine) cause
severe thrombocytopenia.
26. Immune Thrombocytopenia
• Neonatal allo-immune thrombocytopenia
(NAIT)
• Incidental thrombocytopenia of
pregnancy or Gestational
thrombocytopenia
• Autoimmune thrombocytopenic purpura
27. Neonatal allo-immune
thrombocytopenia (NAIT )
• Incompatibility between mother and baby
• Similar to Rh disease
• Antibodies against HPA – 1 (most common)
• In utero bleed can occur
• Manifests with first pregnancy in 50%
• Postnatal : petechiae, purpura
ICH in 10% with sequelae
28. NAIT
• Management – fetal blood sampling and
platelet transfusion or maternal IVIG
• If previous sibling had a significant bleed
• Caesarian section
• In newborn – maternal platelets or HPA
compatible platelets
• IVIG 1gm/k for 2 days or 0.5g/k for 4 days
29. Autoimmune Thrombocytopenia
• Maternal ITP or SLE
• Transplacental transfer of autoantibodies
• Bleeding manifestations are less severe
• ICH occurs in less than 1%
• Platelets at birth, and day 2
• If less than 30,000/cmm – to give IVIG
• Platelet transfusion is not useful
31. TAR (Thrombocytopenia & Absent
Radii)
• Congenital
• Findings
– Thrombocytopenia
– Absent radii bilaterally
– Small shoulders
– Abnormal knees
– Malabsorption
• History
– Platelets stabilize
– ? Leukemia
32. PT and APTT
• PT: measures extrinsic pathway
• VII, X, II, V
• Normal range : preterm:13s(10.6s-16.2s)
term : 13s(10.1-15.9s)
• APTT: Measures intrinsic pathway
• VIII, IX,XI,XII, X,II, V
• Uses a contact activator like kaolin , silica
• Normal values: Term-42.9s(31s-54s)
Preterm – 53.6s( 27.5 – 79s)
33. Thrombin time
• Measures final step of clotting cascade
• Normal values in newborn
• Prolonged in
hypofibrinogenemia, dysfibrinogenemia,
heparin and FDP
• Reptilase time: uses a snake venom
• Not sensitive to heparin
34. Approach in healthy baby
• Plt PT PTT Diagnosis
• ↓ N N ITP , marrow
aplasia
• N ↑ ↑ VKDB
• N N ↑ Clotting defects
• N N N Trauma, XIII
platelet function
35. Approach in sick neonates
• Plt PT PTT Diagnosis
• ↓ ↑ ↑ DIC
• ↓ N N Sepsis, NEC,RVT
• N ↑ ↑ Liver disease
• N N N
Acidosis, hypoxia
36. Bleeding infant
Screening tests
PT, APTT,TT,PLT
BT , Fg, PFA
All tests normal All abnormal
XIII, alpha2- AP APTT prolonged PT prolonged DIC, Liver failure,
PAI, vWFl VIII,IX,XI,XII,vWF VKDB, Warfarin Severe VKDB
hypofg
37. Thank you
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Medical Post [ www.themedicalpost.net ]